NDC 87063-117 – Tramadol Hydrochloride

Tramadol Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CIV

Product NDC87063-117

Product details

Brand name
Tramadol Hydrochloride
Generic name
Tramadol Hydrochloride
Labeler
Asclemed USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA211825
Marketed since
August 9, 2019
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Tramadol Hydrochloride →

Package NDC codes (8)

Package NDCDescriptionSince
87063-117-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-01)Feb 16, 2026
87063-117-05500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-05)Feb 16, 2026
87063-117-1010 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-10)Feb 16, 2026
87063-117-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-20)Feb 16, 2026
87063-117-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-30)Feb 16, 2026
87063-117-5050 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-50)Feb 16, 2026
87063-117-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-60)Feb 16, 2026
87063-117-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-90)Feb 16, 2026

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